Α-Chlorocodide: Difference between revisions
CSV import |
CSV import |
||
| Line 28: | Line 28: | ||
{{pharmacology-stub}} | {{pharmacology-stub}} | ||
<gallery> | |||
File:Alpha-Chlorocodide.svg|Alpha-Chlorocodide | |||
</gallery> | |||
Latest revision as of 20:56, 25 February 2025
Α-Chlorocodide is a synthetic opioid analgesic drug, a derivative of codeine in which the 6-hydroxy group has been replaced by chlorine. Developed in the late 1950s, it has primarily been used in the treatment of moderate to severe pain.
Chemistry[edit]
Α-Chlorocodide is a chlorinated derivative of codeine that has similar pharmacological properties but with a more potent analgesic effect. It is synthesized by reacting codeine with Thionyl chloride, which substitutes a chlorine atom for the 6-hydroxy group.
Pharmacology[edit]
Like other opioids, Α-Chlorocodide acts on the mu-opioid receptors in the brain and spinal cord to relieve pain. It is more potent than codeine and has a similar side effect profile, including respiratory depression, constipation, and dependence.
Clinical Use[edit]
Α-Chlorocodide has been used in the treatment of moderate to severe pain, including post-operative pain, cancer pain, and chronic pain conditions. It is usually administered orally, but can also be given by intramuscular injection.
Side Effects[edit]
The side effects of Α-Chlorocodide are similar to those of other opioids and include drowsiness, dizziness, nausea, vomiting, constipation, and respiratory depression. Long-term use can lead to physical dependence and withdrawal symptoms if the drug is discontinued abruptly.
See Also[edit]
References[edit]
<references />
-
Alpha-Chlorocodide
